| Literature DB >> 32924377 |
Lihua Wang-Eckhardt1, Matthias Eckhardt1.
Abstract
Treatment of different cell lines with progesterone receptor membrane component 1 (PGRMC1) antagonist AG-205 rapidly induces the formation of large vesicular structures that likely represent endosomes. Crispr/Cas9 was used to target the PGRMC1 and progesterone receptor membrane component 2 (PGRMC2) genes in CHO-K1 and HeLa. Unexpectedly, deficiency in one of these or both genes did not inhibit the formation of enlarged vesicles by AG-205, demonstrating additional molecular target(s) of this compound besides PGRMC1. Thus, AG-205 cannot be regarded as a PGRMC1-specific antagonist. However, provided that its currently unknown target(s) will be identified, AG-205 may serve as a new reagent to study endosomal trafficking.Entities:
Keywords: AG-205; membrane associated progesterone receptor family; neudesin; neuferricin
Mesh:
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Year: 2020 PMID: 32924377 DOI: 10.1515/hsz-2019-0417
Source DB: PubMed Journal: Biol Chem ISSN: 1431-6730 Impact factor: 3.915